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BMJ Case Rep. 2021 Mar 10;14(3):e239509. doi: 10.1136/bcr-2020-239509.
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本文引用的文献

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Diagnosis and treatment of acute appendicitis: 2020 update of the WSES Jerusalem guidelines.急性阑尾炎的诊断和治疗:WSES 耶路撒冷指南 2020 年更新版。
World J Emerg Surg. 2020 Apr 15;15(1):27. doi: 10.1186/s13017-020-00306-3.
2
Ileal Cystic Lymphangioma presenting with Acute Appendicitis.表现为急性阑尾炎的回肠囊性淋巴管瘤
J Indian Assoc Pediatr Surg. 2018 Jan-Mar;23(1):36-38. doi: 10.4103/jiaps.JIAPS_44_17.
3
Abdominal lymphatic malformation: Spectrum of imaging findings.腹部淋巴管畸形:影像学表现谱
Indian J Radiol Imaging. 2016 Oct-Dec;26(4):423-428. doi: 10.4103/0971-3026.195777.
4
Abdominal cystic lymphangioma mimicking appendicitis.酷似阑尾炎的腹部囊性淋巴管瘤。
European J Pediatr Surg Rep. 2013 Jun;1(1):32-4. doi: 10.1055/s-0033-1337114. Epub 2013 Mar 20.
5
Surgical management of intra-abdominal cystic lymphangioma. Report of 20 cases.腹腔囊性淋巴管瘤的外科治疗。20 例报告。
World J Surg. 2012 May;36(5):1037-1043. doi: 10.1007/s00268-012-1515-2.
6
Giant mesenteric cystic lymphangioma presenting with abdominal pain and masquerading as a gynecologic malignancy.以腹痛为表现并伪装成妇科恶性肿瘤的巨大肠系膜囊性淋巴管瘤。
Rare Tumors. 2009 Dec 28;1(2):e48. doi: 10.4081/rt.2009.e48.
7
Acquired omental cystic lymphangioma after subtotal gastrectomy: a case report.胃大部切除术后获得性脐疝囊状淋巴管瘤 1 例报告。
J Korean Med Sci. 2009 Dec;24(6):1212-5. doi: 10.3346/jkms.2009.24.6.1212. Epub 2009 Nov 9.
8
Mesenteric lymphangioma in adult: a case series with a review of the literature.成人肠系膜淋巴管瘤:病例系列并文献复习。
Dig Dis Sci. 2009 Dec;54(12):2758-62. doi: 10.1007/s10620-008-0674-3.
9
Giant cystic lymphangioma of pancreas.胰腺巨大囊性淋巴管瘤
ANZ J Surg. 2008 Aug;78(8):673-4. doi: 10.1111/j.1445-2197.2008.04615.x.
10
Mesenteric cystic lymphangioma.肠系膜囊性淋巴管瘤
J Am Coll Surg. 2003 Apr;196(4):598-603. doi: 10.1016/S1072-7515(02)01755-6.

成人囊性淋巴管畸形酷似急性阑尾炎 1 例:罕见的诊断陷阱。

A case of cystic lymphatic malformation mimicking acute appendicitis in an adult patient: a rare diagnostic pitfall.

机构信息

Department of General Surgery, Waitemata District Health Board, Takapuna, New Zealand

Department of General Surgery, Taranaki District Health Board, New Plymouth, New Zealand.

出版信息

BMJ Case Rep. 2021 Mar 10;14(3):e239509. doi: 10.1136/bcr-2020-239509.

DOI:10.1136/bcr-2020-239509
PMID:33692052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7949445/
Abstract

Abdominal cystic lymphatic malformations are rare pathological entities of uncertain aetiology that usually present in early childhood with indolent abdominal distention. We report the case of a 17-year-old man who presented to our hospital with acute right lower quadrant pain, nausea and anorexia. His blood tests revealed a raised white cell count and elevated inflammatory markers. Clinical examination revealed signs of localised right lower quadrant peritonism. A diagnosis of clinical appendicitis was made, and in keeping with local management protocols, the patient proceeded to theatre for a diagnostic laparoscopy without radiological investigations. Operative findings yielded a normal appendix and a large abdominal cystic malformation. This article highlights the need to keep a broad differential diagnosis when performing surgery on patients with clinically presumed appendicitis and the importance of radiological investigations in clinical decision-making, we also review abdominal cystic lymphatic malformations as a rare diagnostic pitfall.

摘要

腹部囊性淋巴管畸形是一种罕见的、病因不明的病理性疾病,通常在儿童早期出现,表现为慢性腹部膨胀。我们报告了一例 17 岁男性患者,因急性右下腹痛、恶心和食欲不振而就诊。他的血液检查显示白细胞计数升高和炎症标志物升高。临床检查显示右下象限局限性腹膜炎的体征。临床诊断为阑尾炎,根据当地管理方案,患者在没有进行放射学检查的情况下进行了诊断性腹腔镜手术。手术结果显示阑尾正常,但有一个大的腹部囊性畸形。本文强调了在对临床诊断为阑尾炎的患者进行手术时需要保持广泛的鉴别诊断,以及放射学检查在临床决策中的重要性,我们还回顾了腹部囊性淋巴管畸形作为一种罕见的诊断陷阱。